SALINE SOLUTION- STERILE
K-Number: K922033 · 1992-07-21
Advertisement
Device Summary
Frequently Asked Questions
What is the SALINE SOLUTION- STERILE?
SALINE SOLUTION- STERILE is a medical device that received FDA 510(k) clearance on 1992-07-21. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K922033.
When did SALINE SOLUTION- STERILE receive FDA 510(k) clearance?
SALINE SOLUTION- STERILE received FDA 510(k) clearance on 1992-07-21, under 510(k) number K922033.
Who is the listed applicant for SALINE SOLUTION- STERILE?
The FDA 510(k) record lists Trinity Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SALINE SOLUTION- STERILE?
The FDA product code for SALINE SOLUTION- STERILE is CCQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Trinity Laboratories, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CCQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement